Data Management STREAM

  1. TMF Migrations: Streamlining The Journey To An Inspection-Ready Result 9/18/2023

    Delve into several techniques designed to safeguard data precision and integrity throughout the TMF migration process, reducing compliance risks and conserving valuable time and effort.

  2. Bench To Market In Record Time With Decentralized Technology 7/6/2021

    How do you develop COVID-19 vaccines and treatments safely in less than a year, virtually? The answer is decentralized technologies, which allows for patient participation outside of the traditional trial site and virtual clinical oversight activities, on a single platform. This session demonstrates how remote data capture linked to real time data insights helps customers get life-saving vaccines and treatments to patients in record time.

  3. Why Veeva CDB 6/24/2024

    Watch a two-minute video to learn how Veeva Clinical Database (CDB) aggregates, cleans, and transforms clinical data from various sources, including third-party EDCs.

  4. How Clinical Data Studio Works Across The Organization 6/19/2024

    Explore how Clinical Data Studio converts data into actionable knowledge, fostering seamless collaboration across teams to enhance the efficiency and effectiveness of clinical trials.

  5. Amplifying Evidence With Unified Clinical Trial Data Collection 5/3/2024

    In this presentation, we explore the transformative potential of integrating a unified clinical trial data collection platform with intelligent automation, challenging the inadequacies of the status quo.

  6. The Many Facets Of Early Phase Evaluation Of Psychedelics In Psychiatry 2/3/2023

    Altasciences and Sygnature Discovery discuss the clinical and non-clinical studies required for evaluation of abuse risks of psychedelic drugs.

  7. Case Study: Optimizing Clinical Supply Chain With Advanced Technology 4/24/2024

    In this interactive discussion, IQVIA Technologies'  IRT experts delve into real-world examples and practical AI applications.

  8. Improving The Quality Of Submitted Studies To ClinicalTrials.gov 11/7/2019

    Want to reduce QC comments? Hear tips from Dr. Deborah Zarin, former director of ClinicalTrials.gov, now with the MRCT Center. Dr. Zarin was keynote speaker at the recent EXTRA: TrialScope Transparency Experience.

  9. The Importance Of Reliable Data To Clinical Trial Activation 5/8/2025

    Find an easier way to identify and enroll eligible patients for your clinical trials with quality data and site selection.

  10. psiXchange: Intelligent, Automated Safety Reporting 3/25/2024

    Say goodbye to manual burdens and embrace efficiency by fully automating your safety reporting. This will significantly cut down on effort and costs, all while enhancing compliance standards.